71 Bioengineering Jobs

Job Title: Environment/Science Journalist Location: Remote Experience Level: 3–7 years Type: Full-Time About LH2 Holdings LH2 Holdings is an AI-powered digital media accelerator and holding company. We acquire or partner with digital media brands (content websites now > youtube channels, social media creators, podcasts, newsletters in the future) and scale them though tech, content and distribution infrastructure. We currently work with ~25 brands across different niches with ~50M monthly pageviews under management wherein each brand has been scaled 3-10x. Our vision is to become the largest distributed digital media company in the world. LH2 is being built by second-time founders who have scaled tech platforms with hundreds of millions of users. About the Role We are hiring a Science Writer for Earth.com who can bridge rigorous scientific research and public understanding. This role requires someone who works at the intersection of science and storytelling, able to transform dense, peer-reviewed research into compelling narratives that spark curiosity and drive understanding. You will write about cutting-edge topics spanning climate science, chemistry, evolutionary biology, genetics, ecology, conservation, sustainability, and emerging technologies. This is not just about summarizing studies; it’s about translating them with accuracy, empathy, and impact. If you’re passionate about science and storytelling and love simplifying complexity without diluting meaning, we’d love to speak to you. Responsibilities Write 2 well-researched, original science articles daily (800–1,200 words each) for a global science-curious audience Translate peer-reviewed studies into engaging, accurate, and accessible content without oversimplification Pitch and develop weekly story ideas from scientific journals, conferences, and global science news Conduct expert interviews with researchers and scientists to enrich reporting with authoritative insights Liaise with editors to refine storytelling, reader engagement, and headline strategies Contribute to fact-checking, copyediting, and multimedia content such as scripts for video explainers Stay on top of breakthroughs in environmental science, chemistry, genetics, climate change, and sustainability Required Qualifications 3–7 years of professional experience in science writing, environmental reporting, or academic/science communication, with published work in reputable outlets strongly preferred Bachelor’s or Master’s degree in a scientific discipline (e.g., Biology, Environmental Science, Chemistry, Bioengineering, Earth Sciences, or related fields); advanced degrees are a plus Proven ability to explain complex scientific concepts in an accurate, engaging, and accessible way for general audiences Strong portfolio of published work (articles, features, explainers, or multimedia) in science, environment, or related fields Skilled in researching, sourcing, and accurately summarizing peer-reviewed studies Strong editorial instincts and attention to detail, with experience in fact-checking, editing, or copyediting scientific content Ability to balance technical precision with narrative-driven storytelling and a reader-first mindset Familiarity with newsroom workflows, content management systems, digital publishing tools, and SEO best practices Knowledge of academic publishing standards, citation formats, and scientific terminology What We Offer Competitive compensation Remote-first role with global reach A chance to work with a high-visibility science brand, read by millions monthly A collaborative editorial environment that values clarity, credibility, and creativity Opportunity to expand into multimedia science communication including scripts, thought leadership, and video content We are not looking for science-focused news writers.

Profile Jivanu Therapeutics Pvt. Ltd is looking for an accomplished and highly motivated Research Scientist to join our R&D team in Bengaluru, Karnataka. This role offers a unique opportunity to contribute to cutting-edge biotechnology research in a rapidly growing and innovation-driven microbiome-based organization. The ideal candidate will have a strong scientific background, hands-on research experience in a biotech or life sciences domain, expertise in the field of microbiome, and a track record of impactful contributions from premier global institutions. Responsibilities Design and implement impactful projects focused on developing microbiome-based products through the creation of novel biotherapeutic bacterial strains and defined consortia. Engage in strain engineering (vector cloning, knockout, knock-in, etc.) and develop in vitro microbiological, biochemical, and biophysical assays to assess the expression and efficacy of the engineered bacteria. Experience with handling anaerobic organisms is strongly preferred. Promote innovation by genetically modifying organisms that are traditionally challenging, which may require novel strategy adoption and lengthy optimization processes. Expected to work on multiple related projects in a startup environment and conceive new ideas. Effectively contribute as a member of a small, multi-functional team by taking initiative and accountability for assigned projects, emphasizing troubleshooting and ensuring timely delivery. Active collaboration with various teams across different domains of expertise, such as bioinformatics, in vivo efficacy, product formulation, etc., is essential. Contribute scientifically by assisting in the preparation of grants, presentations, papers, and patent applications. Qualification Ph.D. in Microbiology, Biotechnology, Molecular Biology, Biochemistry, Bioengineering, or a related field from a premier Indian institution with a strong publication record. Experience Experience conducting impactful translational or applied research in the microbiome and biomedical fields. Demonstrated research excellence through peer-reviewed publications, patents, or technology development. Proven experience in managing or leading scientific projects from conception to execution. Exceptional communication and organizational skills. Preferred Prior experience in genetic engineering, synthetic biology, consortia building. Education or work experience at leading international institutions. Experience working in cross-border or multicultural teams. Familiarity with IP generation, regulatory pathways, or translational research pipelines. To Apply Application Instructions: Please submit your CV, a brief statement of research interests, and contact information for 23 professional references. To apply, please submit a resume/CV and cover letter outlining your qualifications and interest in the position to hr@jivanutx.com. Additionally, provide examples of relevant projects or publications, along with contact information for references.

We at Zenith Quality Assessors Pvt. Ltd. (www.zenith-worldwide.com) are appointing Full Time ISO 13485 Medical Device – Quality Management System Auditors (MD-QMS Auditors). Job Location : Pune, Maharashtra, India Qualification : Bachelor / Master Degree in any of the fields, such as, Biology, Microbiology, Chemistry, Biochemistry, Computer and Software Technology, Electrical, Electronic, Mechanical Engineering, Bioengineering, Human Physiology, Medicine, Pharmacy, Physics or Biophysics Industrial Work Experience in Active Medical Device Industry : 3-4 Years minimum Pre-requisites (Recommended) : Qualified Lead Auditor in ISO 13485:2016 Third Party Audit Experience is preferred. Zenith is accredited by Indian and International Accredited Bodies for providing ISO 13485, ICMED 13485 & other Management Systems certifications, as per applicability. Additionally, Zenith provides audit and certification services for CE Conformity Assessments in co-operation with Internationally recognized EU Notified Bodies or Product Certification Bodies. For more details, please visit our website @ www.zenith-worldwide.com If interested, please write to us with your updated Resume at certification@zenith-worldwide.com alongwith your current and expected CTC. If not relevant to you, will appreciate if you could further share this opportunity to any eligible candidate of your reference

Alien Technology Transfer empowers top-class innovators to transform visionary product concepts into commercial realities. We do this by helping companies with concrete growth ambitions to secure funding for their product development through our innovation consulting expertise. To date, we have raised more than $500 million for our clients - Small and Medium Enterprises (SMEs) - across many domains, including agri-tech, artificial intelligence, biotechnology, clean-tech, cyber-security, quantum computing, space, and transport. We are looking for a Lead Generation Specialist able to source and analyse the highest quality prospect clients for our business lines amongst the most innovative high-tech high-impact start-ups and Small and Medium Enterprises (SMEs) in Europe and the USA. To join the team you have to possess a genuine interest in technology and business, an aptitude in quickly understanding complex engineering or medical innovations, be highly analytical and articulate, and have a strong command of English. You must be a team player, well organized, and also keen to take on responsibility. Key qualities include being able to demonstrate an entrepreneurial mindset, being highly self-motivated, and having a high degree of stamina to work within an ambitious and goal-driven environment. The role will see you undertake the responsibility of scouting potential clients, mainly by leveraging digital resources and channels (search engines, industry websites, and events), and by analyzing various databases (implying also some software programming tasks). DUTIES AND RESPONSIBILITIES Keeping yourself continuously up to date in the technological and business field to quickly and effectively recognize business opportunities and industry/market emerging trends Continuously identifying top-level sources/hubs of potential clients among web platforms, online databases, and events (trade fairs, conferences, pitches, start-up competitions, etc) Monitoring current trends in private and public innovative project financing and fund-raising Handling and analyzing databases, including any applicable customized filtering option to deliver the most appropriate results Analyzing and critically evaluating information resulting from any search related to innovative technologies and businesses Maintaining and enriching internal databases for prospects, clients, and public grant awardees. Preparing regular reports on funding trends, requiring quantitative skills, which help define the company’s yearly targets. JOB REQUIREMENTS Must have at least a Master’s degree in Life Science (Bioengineering, Biomedical, Biotechnology, Neurosciences, Biochemistry, Microbiology, etc...) Advanced use of Excel and aptitude to master the use of professional industry database Proficiency in using digital resources (e.g. search engines) to uncover new leads Self-starting, inquisitive, and pragmatic attitude Fluent English comprehension, oral and written Knowledge of Python programming for web scraping/extraction mechanisms is a plus. An added advantage if has an idea for the creation of web scrapers for extracting startup data from different websites supporting the development of a startup Lead Generation. Please note: Due to the high volume of candidates we are unfortunately not able to provide individual feedback regarding the outcome of every single application.

Job Title: Scientist – Lateral Flow Assay (LFA) Location: Parwanoo, Himachal Pradesh Experience Required: 3–9 Years Notice Period: Immediate to 30 Days Total Experience: 3–9 Years Education :- Master’s or Ph.D. in Biotechnology, Biochemistry, Bioengineering, Analytical Chemistry , or a closely related scientific discipline. Technical Expertise :- End-to-end expertise in LFA development from concept through validation. Advanced experience in nanoparticle bioconjugation (especially gold nanoparticles ), including fabrication, characterization, and stability studies. Ability to troubleshoot LFA performance issues (low signal, high background, flow irregularities, long-term stability). Strong understanding of LFA materials (nitrocellulose membranes, conjugate pads, sample pads) and their influence on performance. Skilled in Design of Experiments (DoE) and statistical analysis for assay optimization. Familiarity with manufacturing processes and scale-up for LFAs. Preferred Qualifications :- Experience in developing LFAs for whole blood samples , including on-board buffer integration . Understanding of regulatory requirements for IVD product development (e.g., ISO 13485). Experience with advanced nanoparticle characterization techniques: Dynamic Light Scattering (DLS) Zeta Potential Transmission Electron Microscopy (TEM) UV-Vis Spectroscopy Skills & Abilities :- Highly analytical and detail-oriented with strong problem-solving capabilities. Ability to design, execute, and interpret experiments independently. Excellent scientific writing skills for reports, publications, and regulatory documentation. Strong verbal communication and presentation abilities for internal and external stakeholders. Collaborative mindset with proven ability to work across cross-functional teams. Job Type: Full-time Work Location: In person

Job Title: Scientist – Lateral Flow Assay (LFA) Location: Parwanoo, Himachal Pradesh Experience Required: 3–9 Years Notice Period: Immediate to 30 Days Total Experience: 3–9 Years Education :- Master’s or Ph.D. in Biotechnology, Biochemistry, Bioengineering, Analytical Chemistry , or a closely related scientific discipline. Technical Expertise :- End-to-end expertise in LFA development from concept through validation. Advanced experience in nanoparticle bioconjugation (especially gold nanoparticles ), including fabrication, characterization, and stability studies. Ability to troubleshoot LFA performance issues (low signal, high background, flow irregularities, long-term stability). Strong understanding of LFA materials (nitrocellulose membranes, conjugate pads, sample pads) and their influence on performance. Skilled in Design of Experiments (DoE) and statistical analysis for assay optimization. Familiarity with manufacturing processes and scale-up for LFAs. Preferred Qualifications :- Experience in developing LFAs for whole blood samples , including on-board buffer integration . Understanding of regulatory requirements for IVD product development (e.g., ISO 13485). Experience with advanced nanoparticle characterization techniques: Dynamic Light Scattering (DLS) Zeta Potential Transmission Electron Microscopy (TEM) UV-Vis Spectroscopy Skills & Abilities :- Highly analytical and detail-oriented with strong problem-solving capabilities. Ability to design, execute, and interpret experiments independently. Excellent scientific writing skills for reports, publications, and regulatory documentation. Strong verbal communication and presentation abilities for internal and external stakeholders. Collaborative mindset with proven ability to work across cross-functional teams. Job Type: Full-time Work Location: In person

About Velsera Medicine moves too slow. At Velsera, we are changing that. Velsera was formed in 2023 through the shared vision of Seven Bridges and Pierian, with a mission to accelerate the discovery, development, and delivery of life-changing insights. Velsera provides software and professional services for: AI-powered multimodal data harmonization and analytics for drug discovery and development IVD development, validation, and regulatory approval Clinical NGS interpretation, reporting, and adoption With our headquarters in Boston, MA, we are growing and expanding our teams located in different countries! What will you do? Lead the design, development, and implementation of bioinformatics solutions for analyzing and managing biological data using Python, while adhering to best practices and quality standards. Collaborate with research scientists, software engineers, clinical teams, and external stakeholders to design bioinformatics workflows for ongoing projects and to build bioinformatics solutions. Foster a collaborative, innovative, and inclusive team culture that encourages continuous learning and knowledge sharing Identify and/or conceive novel approaches to better and more efficiently analyze client and public datasets. Participate in defining the high-level application architecture for future roadmap requirements and features. Coach team members by sharing domain and technical knowledge and code reviews. Drive improvements in quality assurance processes, addressing bottlenecks and inefficiencies to optimize workflows. Participate in activities such as hiring and onboarding. Work with cross-functional teams to ensure quality throughout the bioinformatics software and analytical pipelines development lifecycle. Exceptional problem-solving abilities and a passion for translating complex biological questions into actionable computational solutions. Ability to work under pressure and manage multiple projects simultaneously. Ensure compliance with our SDLC process during product development. Stay up-to-date on technology to deliver quality at each phase of the product life-cycle. You take leadership in evangelizing technical excellence within the team. Requirements What do you bring to the table? Ph.D. degree with 8+ years of postdoc or industrial experience or Masters Degree with 10+ years of industrial experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology or related field with atleast 3+ years experience in leadership or managerial role. Extensive experience with bioinformatics tools, pipelines, and algorithms for genomics data analysis. Strong understanding of genomic data analysis, variant calling, targeted, whole-exome and whole-genome analysis. Excellent programming skills in Python and Shell scripting. Experience with Relational database such as PostgreSQL, mySQL or Oracle. Experience with version control systems such as GitHub. Experience with Linux/UNIX/Mac OS X based systems Experience with high-performance Linux cluster and cloud computing (AWS is preferred). Deep understanding of analytical approaches and tools for genomic data analysis along with familiarity with genomic databases. Candidates with proven expertise in the analysis of NGS data generated on sequencing platforms such as Illumina, Oxford Nanopore, or Thermo will be prioritized. Experience with open source bioinformatics tools and publicly available variant databases. Ability to manage moderately complex projects and initiatives. Exceptionally strong communication, data presentation and visualization skills. Personal initiative and ability to work effectively with in a cross functional team. Excellent communication skills and ability to learn and work independently when necessary. High energy and inquisitive and strong attention to detail. Benefits Flexible Work & Time Off - Embrace hybrid work models and enjoy the freedom of unlimited paid time off to support work-life balance. Health & Well-being - Access comprehensive group medical and life insurance coverage, along with a 24/7 Employee Assistance Program (EAP) for mental health and wellness support. Growth & Learning - Fuel your professional journey with continuous learning and development programs designed to help you upskill and grow. Recognition & Rewards - Get recognized for your contributions through structured reward programs and campaigns. Engaging & Fun Work Culture - Experience a vibrant workplace with team events, celebrations, and engaging activities that make every workday enjoyable. & Many More...

🔬 Hiring: Senior Scientist – Crop Modeling (GHG & Carbon Analytics) 📍 Location: Delhi-NCR | 🕒 Full-Time | 🌿 Domain: Sustainable Agriculture & Climate Science 💰 Budget: Up to ₹60 LPA We’re looking for a seasoned scientist to lead carbon and GHG quantification efforts using advanced crop modeling tools. This role demands deep expertise in biogeochemical modeling, agronomic systems, and climate-smart analytics. 🔍 Role Highlights: Apply biogeochemical models to quantify GHG emissions from agricultural practices Build and manage databases tailored to model-specific input requirements Evaluate model applicability across diverse Indian agro-climatic zones Generate comparative insights and decision-support tools for internal teams Support regenerative agriculture and soil health initiatives through data-driven modeling 🎓 Qualifications: PhD in Environmental/Agricultural Sciences, Bioengineering, or related field 8–12 years of experience in crop modeling, GHG quantification, and biostatistics Strong grasp of agricultural practices and mathematical modeling Proficient in MS Office and analytical tools; exposure to data science preferred Excellent communication and problem-solving skills 🛠️ Must-Have Expertise: Biogeochemical modeling (DNDC, DayCent, APSIM) GHG quantification frameworks and modeling tools Crop modeling, emissions tracking, and statistical analysis Familiarity with regenerative and climate-resilient farming systems

About Velsera Medicine moves too slow. At Velsera, we are changing that. Velsera was formed in 2023 through the shared vision of Seven Bridges and Pierian, with a mission to accelerate the discovery, development, and delivery of life-changing insights. Velsera provides software and professional services for: AI-powered multimodal data harmonization and analytics for drug discovery and development IVD development, validation, and regulatory approval Clinical NGS interpretation, reporting, and adoption With our headquarters in Boston, MA, we are growing and expanding our teams located in different countries! What will you do? Lead the design, development, and implementation of bioinformatics solutions for analyzing and managing biological data using Python, while adhering to best practices and quality standards. Collaborate with research scientists, software engineers, clinical teams, and external stakeholders to design bioinformatics workflows for ongoing projects and to build bioinformatics solutions Foster a collaborative, innovative, and inclusive team culture that encourages continuous learning and knowledge sharing Identify and/or conceive novel approaches to better and more efficiently analyze client and public datasets. Participate in defining the high-level application architecture for future roadmap requirements and features. Coach team members by sharing domain and technical knowledge and code reviews. Drive improvements in quality assurance processes, addressing bottlenecks and inefficiencies to optimize workflows. Participate in activities such as hiring and onboarding. Work with cross-functional teams to ensure quality throughout the bioinformatics software and analytical pipelines development lifecycle. Exceptional problem-solving abilities and a passion for translating complex biological questions into actionable computational solutions. Ability to work under pressure and manage multiple projects simultaneously. Ensure compliance with our SDLC process during product development. Stay up-to-date on technology to deliver quality at each phase of the product life-cycle. You take leadership in evangelizing technical excellence within the team. Requirements What do you bring to the table? Ph.D. degree with 8+ years of postdoc or industrial experience or Masters Degree with 10+ years of industrial experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology or related field with atleast 3+ years experience in leadership or managerial role. Extensive experience with bioinformatics tools, pipelines, and algorithms for genomics data analysis. Strong understanding of genomic data analysis, variant calling, targeted, whole-exome and whole-genome analysis. Excellent programming skills in Python and Shell scripting. Experience with Relational database such as PostgreSQL, mySQL or Oracle. Experience with version control systems such as GitHub. Experience with Linux/UNIX/Mac OS X based systems Experience with high-performance Linux cluster and cloud computing (AWS is preferred). Deep understanding of analytical approaches and tools for genomic data analysis along with familiarity with genomic databases. Candidates with proven expertise in the analysis of NGS data generated on sequencing platforms such as Illumina, Oxford Nanopore, or Thermo will be prioritized. Experience with open source bioinformatics tools and publicly available variant databases. Ability to manage moderately complex projects and initiatives. Exceptionally strong communication, data presentation and visualization skills. Personal initiative and ability to work effectively with in a cross functional team. Excellent communication skills and ability to learn and work independently when necessary. High energy and inquisitive and strong attention to detail. Benefits Flexible Work & Time Off - Embrace hybrid work models and enjoy the freedom of unlimited paid time off to support work-life balance Health & Well-being - Access comprehensive group medical and life insurance coverage, along with a 24/7 Employee Assistance Program (EAP) for mental health and wellness support Growth & Learning - Fuel your professional journey with continuous learning and development programs designed to help you upskill and grow Recognition & Rewards - Get recognized for your contributions through structured reward programs and campaigns Engaging & Fun Work Culture - Experience a vibrant workplace with team events, celebrations, and engaging activities that make every workday enjoyable & Many More..

Job Title: Lateral Flow Assay (Scientist) Location: Parwanoo, Himachal Pradesh, India Job Summary We are seeking a highly motivated and experienced Scientist with deep, hands-on expertise in Lateral Flow Assay (LFA) development to join the R&D team. The successful candidate will be instrumental in driving the design, optimization, and validation of novel LFA products from concept through to commercialization. This role requires a strong analytical mindset, exceptional problem-solving skills, and a genuine passion for pushing the boundaries of rapid diagnostics. Key Responsibilities: LFA Development & Optimization: Lead the design and execution of experiments for all stages of LFA development, including reagent selection, nanoparticle conjugation (especially gold nanoparticles), conjugate pad preparation, membrane selection, and strip assembly. Performance Enhancement: Systematically optimize LFA performance parameters (sensitivity, specificity, robustness, stability, flow characteristics) to meet stringent product requirements. Advanced Troubleshooting: Act as a primary technical expert for diagnosing and resolving complex LFA performance issues such as inconsistent signal, high background, poor flow, and long-term stability challenges (e.g., conjugate degradation, batch variability). Component Characterization: Conduct thorough characterization of critical LFA raw materials (nanoparticles, antibodies, membranes, pads) and in-process intermediates to ensure quality and performance. QC & Validation: Develop and implement robust quality control methods for LFA components and finished devices. Contribute significantly to analytical validation studies (LoD, LoQ, specificity, stability, reproducibility). Data Analysis & Documentation: Design rigorous experiments (including DoE), analyze complex data using statistical tools, and maintain meticulous laboratory records and documentation. Cross-functional Collaboration: Work closely with manufacturing, quality assurance, and regulatory teams to facilitate seamless design transfer and scale-up of LFA products. Required Qualifications Education: Master’s or Ph.D. in Biotechnology, Biochemistry, Bioengineering, Analytical Chemistry, or a closely related scientific discipline. Experience: Minimum of 2–3+ years of hands-on, direct LFA development experience in academia, IVD, or the medical device industry. Technical Expertise: Demonstrated proficiency in all aspects of LFA development from conception to validation. Expert-level hands-on experience with nanoparticle bioconjugation, particularly gold nanoparticles, including nanoparticle fabrication, characterization, and stability assessment. Proven ability to troubleshoot complex LFA performance issues (e.g., low signal, high background, flow inconsistencies, long-term stability). Strong understanding of various LFA materials (nitrocellulose membranes, conjugate pads, sample pads) and their impact on assay performance. Proficiency in experimental design (DoE) and statistical analysis for LFA optimization. Experience with LFA manufacturing considerations and process scale-up. Analytical Skills: Highly analytical, logical, with strong problem-solving aptitude and meticulous attention to detail. Communication: Excellent written and verbal communication skills; ability to present complex scientific data clearly and concisely. Preferred Qualifications Experience developing LFAs for whole blood samples, including on-board buffer integration. Familiarity with regulatory guidelines relevant to IVD product development (e.g., ISO 13485). Experience with advanced analytical techniques for characterizing nanoparticles (e.g., DLS, Zeta Potential, TEM, UV-Vis Spectroscopy). Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,800,000.00 per year Work Location: In person

Job Title: Lateral Flow Assay (Scientist) Location: Parwanoo, Himachal Pradesh, India Job Summary We are seeking a highly motivated and experienced Scientist with deep, hands-on expertise in Lateral Flow Assay (LFA) development to join the R&D team. The successful candidate will be instrumental in driving the design, optimization, and validation of novel LFA products from concept through to commercialization. This role requires a strong analytical mindset, exceptional problem-solving skills, and a genuine passion for pushing the boundaries of rapid diagnostics. Key Responsibilities: LFA Development & Optimization: Lead the design and execution of experiments for all stages of LFA development, including reagent selection, nanoparticle conjugation (especially gold nanoparticles), conjugate pad preparation, membrane selection, and strip assembly. Performance Enhancement: Systematically optimize LFA performance parameters (sensitivity, specificity, robustness, stability, flow characteristics) to meet stringent product requirements. Advanced Troubleshooting: Act as a primary technical expert for diagnosing and resolving complex LFA performance issues such as inconsistent signal, high background, poor flow, and long-term stability challenges (e.g., conjugate degradation, batch variability). Component Characterization: Conduct thorough characterization of critical LFA raw materials (nanoparticles, antibodies, membranes, pads) and in-process intermediates to ensure quality and performance. QC & Validation: Develop and implement robust quality control methods for LFA components and finished devices. Contribute significantly to analytical validation studies (LoD, LoQ, specificity, stability, reproducibility). Data Analysis & Documentation: Design rigorous experiments (including DoE), analyze complex data using statistical tools, and maintain meticulous laboratory records and documentation. Cross-functional Collaboration: Work closely with manufacturing, quality assurance, and regulatory teams to facilitate seamless design transfer and scale-up of LFA products. Required Qualifications Education: Master’s or Ph.D. in Biotechnology, Biochemistry, Bioengineering, Analytical Chemistry, or a closely related scientific discipline. Experience: Minimum of 2–3+ years of hands-on, direct LFA development experience in academia, IVD, or the medical device industry. Technical Expertise: Demonstrated proficiency in all aspects of LFA development from conception to validation. Expert-level hands-on experience with nanoparticle bioconjugation, particularly gold nanoparticles, including nanoparticle fabrication, characterization, and stability assessment. Proven ability to troubleshoot complex LFA performance issues (e.g., low signal, high background, flow inconsistencies, long-term stability). Strong understanding of various LFA materials (nitrocellulose membranes, conjugate pads, sample pads) and their impact on assay performance. Proficiency in experimental design (DoE) and statistical analysis for LFA optimization. Experience with LFA manufacturing considerations and process scale-up. Analytical Skills: Highly analytical, logical, with strong problem-solving aptitude and meticulous attention to detail. Communication: Excellent written and verbal communication skills; ability to present complex scientific data clearly and concisely. Preferred Qualifications Experience developing LFAs for whole blood samples, including on-board buffer integration. Familiarity with regulatory guidelines relevant to IVD product development (e.g., ISO 13485). Experience with advanced analytical techniques for characterizing nanoparticles (e.g., DLS, Zeta Potential, TEM, UV-Vis Spectroscopy). Job Type: Full-time Pay: ₹1,000,000.00 - ₹1,800,000.00 per year Work Location: In person

Product Development Engineer – Medical Devices (Spine) About Indius Medical Technologies : Indius Medical Technologies is an innovative spine-focused medical device company based in Pune, bringing ideas from concept to commercialization with a rigorous quality system and deep surgeon collaboration. Join a fast-paced, high-energy team shaping next‑generation implants and instruments for better patient outcomes. Role overview : The Product Development Engineer owns the full product lifecycle—from concept, design, and prototyping to verification/validation, manufacturing transfer, regulatory readiness, launch, and post‑market support. The role is highly cross‑functional with close engagement with surgeons, test labs, operations, and marketing to deliver high‑quality, on‑time releases. Key responsibilities : · Design and develop spinal implants and surgical instruments using PTC Creo, delivering robust models, drawings, and BOMs that meet clinical and functional requirements. · Translate surgeon and market feedback into clear specifications and risk‑based requirements for new products and line extensions. · Drive rapid prototyping with in‑house and external partners; iterate designs based on test and user feedback. · Plan and execute design verification and validation (bench tests, cadaver labs, functional evaluations) with internal test engineers and accredited labs. · Build and maintain Design History Files (DHF), project plans, and documentation in full compliance with Indian CDSCO, US FDA expectations. · Partner with operations to establish manufacturing routes, fixtures, and supplier readiness; support sourcing and cost‑down activities. · Collaborate with marketing on forecasts, launch plans, and sales training; provide early field support and post‑launch monitoring to drive continuous improvement. · Continuously research market and competitive technologies to inform innovative design and portfolio strategy. Qualifications · 3–5 years of mechanical product design and development experience, preferably in medical devices; strong mechanical aptitude and hands‑on problem solving. · Bachelor’s in Mechanical, Biomedical Engineering, or Bioengineering (focus on Product/Mechanical Design or Biomechanics); a Master’s in Mechanical/Biomedical/Bioengineering may substitute 2 years’ experience, ideally with Biomechanics/Mechanical Design focus. · Proficiency in 3D CAD (Pro/E/Creo) and sound understanding of DFM/DFA, tolerance stacks, materials, and test methods. · Proficiency in Microsoft Office; familiarity with MS Project or demonstrated project management skills preferred. Ways of working · Proactive, organized, detail‑oriented team player who thrives in a fast‑paced, multi‑project environment and meets deadlines with accountability. · Passion for healthcare and applying engineering rigor to solve real surgical needs; willingness to attend surgeries and labs for product support and validation. · Ability to travel 10–15% as required for suppliers, labs, and field activities. Why join us · Work closely with leading spine surgeons to translate unmet needs into cutting‑edge solutions that reach the market quickly and responsibly. · Own end‑to‑end product impact in a collaborative culture with strong quality systems and growth opportunities in a scaling organization. Location · Pune (Office: Unit No. 12, Electronic Cooperative Estate, Pune–Satara Road, Pune 411009, MH, India) 

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Radiometer, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Radiometer, life comes first. Our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses. As a global leader and pioneer in acute care diagnostics for over 70 years, we streamline diagnostic workflows, empowering healthcare professionals to focus on what truly matters—caring for critically ill patients. We’re a team that celebrates diverse ideas and continuous improvement. Here, you’ll find a place to grow and make a real impact with your unique perspective, driving us forward in improving patient care. Learn about the Danaher Business System which makes everything possible. As part of our strategic expansion and increased capacity at our India site, we are establishing a new team and are currently seeking a Verification & Validation Engineer to take on a pivotal role—combining technical expertise with team leadership responsibilities. In this role, you will lead a small team of lab technicians and be accountable for the integration, verification, and system performance validation of Radiometer products. You will also oversee the planning and execution of activities within our dedicated lab facility, ensuring high standards of quality and compliance. If you are passionate about working with complex systems and bring experience in the verification, validation, and testing of medical devices, this is a unique opportunity to make a significant impact in a dynamic and growing environment. This position reports to the R&D Director, ACDx Systems Releases Department and is part of the Bangalore Development Center located in Bangalore, India. The role is designated as full-time, on-site. In this dynamic and impactful role, you will have the opportunity to: Collaborate with cross-functional development teams to ensure products meet rigorous performance and compliance standards. Design and implement robust verification strategies and plans, balancing quality, risk, and cost-effectiveness. Author verification and validation protocols, conduct thorough data analysis, and compile comprehensive reports aligned with global regulatory standards. Monitor and follow up on test results, providing timely updates and insights to project managers and leadership. Establish and maintain local quality control and assurance procedures in alignment with regional regulatory requirements, in collaboration with RA and QA departments. Lead and manage a team of lab technicians, prioritizing and supervising daily activities within the verification and validation lab. Work in close coordination with the Verification & Validation teams at headquarters to ensure a seamless transfer of capabilities and best practices. The essential requirements of the job include: 6+ years of work experience in Systems Engineering; Work experience in Verification & Validation in Medical devices or in a regulated business; Master in bio-chemistry/molecular biology/biotechnology/bioengineering/biomedical engineering or equivalent; Good knowledge in statistics and in the use of statistic methods; Ability to travel: o ~ 2 months/year to the head quarter in Copenhagen o To the Radiometer site IDC in Bangalore (1-2 times/month) It would be a plus if you also possess previous experience in: Visual agile planning Working with blood in a lab environment Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.

Garuda3D is a leading in-house manufacturer of affordable 3D printers in India, specializing in FFF & SSE (Food & Bio) 3D printing technology. With over 8.3 years of experience, our team of professionals produces a wide variety of large format 3D printers that cater to both professional and industrial applications. We are now developing Bio3d printers. For that, we're seeking a highly motivated Biomedical Engineering Intern to join our team! We're looking for a talented and enthusiastic Biomedical Engineering Intern to contribute to our bio 3D printing project. As an intern, you will have the opportunity to work on exciting Bio 3d printing projects, collaborate with our team, and gain hands-on experience in bio 3D printing. Roles and Responsibilities: - Research and understand Bio 3D printing technologies, materials, and applications - Assist in designing and developing Bio 3D printing experiments - Conduct literature reviews and analyze data related to Bio 3D printing - Assist in writing proposals and reports - Collaborate with our team to achieve project goals and objectives - Develop and present project updates and findings to the team Requirements: - A degree in Biomedical Engineering, Bioengineering, Biotechnology, Pharmaceutical, or related field - Strong understanding of Bio 3D printing principles, materials, and applications - Knowledge in Tissue Engineering and Cell culture - Knowledge in Bio fabrication and Bio mechanics - Experience in Biomimetics This is a paid Internship with a stipend between Rs.10000 - Rs.12000 Internship duration is 6 months,

You will be working as a Junior Research Fellow/Research Assistant for a project focusing on the evaluation of the role of exovesicles in neural development and leukemias. The position is set to commence on 1st June 2025 with one vacancy available. The salary will be as per the Research fellowship scale sanctioned by the grant, and proficiency in English is required. Ideal candidates should have experience in model system research or wet lab experience in cellular or molecular biology, or bioengineering. Freshers with fellowships will also be considered. A Master's degree in areas related to biology, bioengineering, medical biotechnology, or life sciences disciplines is preferred. Your responsibilities will include designing and conducting experiments to evaluate the molecular mechanisms of therapy resistance in leukemias or neuronal patterning. You will coordinate with various research teams and departments, assist in lab management tasks such as ordering consumables and maintaining lab records, and analyze findings related to disease conditions and developmental models. Additionally, you will be involved in manuscript writing and participating in academic and scientific activities. Interested candidates are required to submit their resume to the Principal Investigator of the SERB COMP 2023 project at SJRI via email. The application deadline is 24th May 2025. Please include a cover letter, curriculum vitae, and 3 references. For more details and to apply, visit the website www.sjri.res.in or contact the provided phone numbers 080-49467010/49467011.,

Date: 18 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Upstream Process Development Scientist We're looking for an Upstream Process Development Scientist with 2-5 years of experience to join our team. In this role, you'll be crucial in developing and optimizing upstream processes for the production of large molecules, including monoclonal antibodies (mAbs) and biosimilars. If you have a strong background in handling CHO cells and experience with cutting-edge bioreactor systems, we encourage you to apply! Responsibilities Design, execute, and analyze experiments for the development and optimization of upstream cell culture processes, focusing on CHO cell lines. Work with large molecules, including monoclonal antibodies (mAbs) and biosimilars, throughout the process development lifecycle. Operate and troubleshoot various bioreactor systems, including AMBR250, Single-Use Bioreactors (SUBs), and 10L reactors. Optimize cell culture media, feeding strategies, and process parameters to maximize yield and product quality. Analyze process data, interpret results, and present findings to the team. Contribute to the transfer of developed processes to manufacturing. Maintain detailed and accurate documentation of all experimental work. Stay current with industry trends and advancements in upstream process development. Qualifications Master's in Chemical Engineering, Biotechnology, Bioengineering, or a related scientific discipline. 2-5 years of hands-on experience in upstream process development within the biopharmaceutical industry. Demonstrated expertise in handling and culturing CHO cells. Proven experience with large molecule production, specifically monoclonal antibodies (mAbs) and biosimilars. Hands-on experience operating and troubleshooting AMBR250, Single-Use Bioreactors (SUBs), and 10L reactors. Strong understanding of cell culture principles, bioreactor operations, and process scale-up. Excellent data analysis, troubleshooting, and problem-solving skills. Ability to work independently and collaboratively in a fast-paced environment. Strong written and verbal communication skills. Bonus Points If You Have Experience with Design of Experiments (DoE) software and statistical analysis. Knowledge of GMP principles and regulatory guidelines

Plaksha University Location Plaksha University, Mohali, Punjab Open Date Sep 13, 2022 Description The Plaksha Research Fellowship (PRF) aims to recruit brilliant fellows in the filed of engineering, applied sciences, and social sciences, who are interested in building a research career at the cutting edge of technology and associated interdisciplinary areas. Research Fellows will be exposed to emerging challenges in research which will lead to the evolution of their research leadership at an international level. They will work under the mentorship of a team of reputed faculty within Plaksha as an integral member of a research lab while collaborating with peers in partner institutions including universities, research laboratories, and industry. Research Fellows will be selected based on their research interests, talent for innovation, and drive to make an impact. We are looking for candidates who are keen to take up intellectual challenges with an eye toward building novel artefacts, devices, and systems, investigating the interface between technology and society, and solving real-life problems. The candidates will get a stipend competitive with the industry, along with an annual grant to attend international conferences/workshops. We expect the Research Fellows to evolve and be an integral part of globally reputed research programs within a short time. We will also strive to offer a suitable environment for the growth of entrepreneurial skills and vision. Responsibilities In the capacity of PRF, you will be required to assist your faculty supervisor in conducting research as well as teaching-related activities. This will include, but is not limited to, the following tasks: Undertaking research in respective areas Writing research and conference papers under the assistance of the faculty. Set up and manage laboratory and project work Assisting faculty in conducting research projects that may involve fabrication, prototyping or programming activities. Interaction with vendors, suppliers, research institutions and related entities on academics and research-related matters Assisting faculty in teaching courses, which may involve 20 hours of work every week. This will involve working with faculty to plan and administer lectures, conducting tutorial and laboratory classes, developing homework problems, performing student assessments, and evaluating quizzes and examination sheets. Compensation and benefits Consolidated monthly stipend of INR 50,000 Medical insurance coverage of INR 5 lac. Travel/conference allowance of up to INR 40,000 per year for attending conferences/workshops. An on-campus residence facility may be provided subject to availability and at cost Contract duration - 6 months or a One-year contract Renewal of contract - The contract can be renewed once upon successful completion of the first term Additional career benefits Priority consideration for admission to the Ph.D. programs at Plaksha based on an excellent performance. Priority consideration for full-time research engineer positions at Plaksha’s research centres based on an excellent performance. Mentorship and guidance in future career trajectories in academia and industry. Qualifications Eligibility criteria Open to brilliant individuals desirous of starting their career in academia. The fellowship is very selective and only those who have a genuine interest in pursuing research and building a career in technological leadership will be selected. Requirements include: Master's degree or equivalent in computer science/ engineering, electrical and electronics engineering, mechanical engineering, bioengineering, mathematics, physics, biology and natural sciences, engineering education, humanities and liberal arts or related areas. Exceptional candidates with only a Bachelor's degree may be considered Research interests should preferably align with our thrust areas such as machine learning, artificial intelligence, data science, robotics and cyber-physical systems, sensors, IoT, biological systems, bioinformatics, engineering ethics, genetic engineering, applied mathematics and humanities among others. For more details and specific areas of faculty research interests, please click here. The candidate should be below 30 years of age. Application Instructions Applications can be submitted by filling out the online form. Along with the form, applicants should send their: (1) CV (2) Statement of Interest (3) Passport size photograph (4) Copy of academic records, work experience (if any) and identity proof Those applicants who meet the eligibility criteria and are found relevant for the PRF position will have to appear for an online written admission test. Applicants shortlisted after the test will be called for an interview. For more information or questions, contact us via email at phd.academics@plaksha.edu.in

About Client : Our is Client is a largest Top 5 Software giant in India, with over 11.3 USD billion dollars revenue, Global work force 2,40,000 employees, It delivers end-to-end technology, consulting, and business process services to clients across the globe, Presence: 60+ countries and Publicly traded company NSE & BSE (India), NYSE (USA). Job Title: Technical Program Manager Exp: 2+ to 5 years Location: Pune Salary: As per market Notice Period: 0-15/serving Technical Program Manager I/II : JD Program Management Team/Bioinformatics BU (Full Time Employment) Excelra is looking for highly skilled and motivated members for the Program Management Team with technical experience across multiple domains (AI/ML,NGS/human genetics/statistics, software development, project management, agile methodology) in bioinformatics to join the Bioinformatics team. The successful candidate will be expected to demonstrate the following competencies: 1.Project management as well as program management across different projects in key client accounts. 2.Liaison the relationship between client and Excelra 3.Contribute to efforts to increase operational efficiency among projects. 4.Collaboration with delivery for successful delivery of projects 5.Interact with the technical stakeholders of clients to identify new business opportunities. Qualifications: • PhD with 2-3 years of industrial experience or M.Sc/M.Tech with 5+ years’ experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology, or related field. • Strong track record of omics (NGS) data analysis, scRNA-Seq analysis or ML/AI and downstream systematic interpretation are must. • Expertise in one or more programming/scripting languages such as R, Python, shell-script for complex data analysis. • Experience in image analysis, knowledge graphs, deep learning and/or LLM’s is an advantage. • Some experience in data engineering techniques, full-stack development is expected. • Understanding of current best practices in computational biology data-management (NGS/Transcriptiomics/Microarray/Proteomics/Clinical-trials/Text-mining, etc.) is an added advantage. • Experience with Docker, Linux environment or cloud computing (AWS/GCP) is a plus. • Experience with Relational database such as Postgres, MySQL, or Oracle, is a plus. • Experience with version control systems such as GitHub, is a plus. • Ability to generate in-silico experimental workflows and in-depth knowledge in proprietary and public biological databases, methods, and tools. • Ability to generate scientific hypothesis along with good scientific/technical communication skills would be preferred

Qualifications: Bachelor’s degree/ Diploma in Biomedical Engineering, Bioengineering, or a related engineering discipline. Experience in medical equipment maintenance, calibration, and troubleshooting preferred. Good communication and teamwork skills with an ability to work collaboratively with clinical staff. Relevant certifications or licenses Scope of Work: Manage, maintain, and repair hospital biomedical equipment to ensure reliability and safety. Collaborate with medical staff to support the proper use and integration of medical devices. Assist in the installation and commissioning of new medical equipment. Conduct periodic inspections and preventive maintenance on diagnostic and therapeutic devices. Provide technical training and support to healthcare professionals on equipment operation. Ensure compliance with regulatory standards and hospital safety protocols. Participate in procurement and evaluation of medical devices and technologies. Contribute to clinical research and innovation related to biomedical technologies Experience: 3+ years in hospital /healthcare setup Salary: As per best industry practices, depending on qualification & experience Urgent requirement, Spot hiring possible Job Type: Full-time Pay: ₹20,000.00 - ₹60,000.00 per month Work Location: In person

Location: Parwanoo, Himachal Pradesh We’re looking for a Scientist (2–3+ yrs experience) with hands-on expertise in LFA development to lead R&D efforts from concept to commercialization. 🔬 Key Responsibilities: End-to-end LFA development & optimization Gold nanoparticle conjugation & troubleshooting Assay validation, data analysis (DoE), and scale-up support Collaboration with QA, RA, and manufacturing teams 🎓 Qualifications: M.Sc ./Ph.D. in Biotech, Biochemistry, Bioengineering or related Strong background in LFA materials, QC, and diagnostics ✨ Bonus: Experience with whole blood LFAs & ISO 13485 🔗 Learn more: https://truehb.com 📩 Apply at: anchal.sharma@wrig.in

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Role Bioproduction Group, Purification and Pharma Analytics division is seeking a motivated and dedicated protein purification Field Application scientist to support Poros and CaptureSelect (CS) resin design in, optimization and troubleshooting at Downstream purification and process development primarily for novel therapeutic monoclonal antibody products including bispecifics, Vaccines and general bioprocessing throughout all stages of clinical trials at key bioprocessing customer sites in India. Responsibility Conduct routine Knowledge culture seminars to highlight Poros and CS resin technology and application at key customer sites Initiate and support customer evaluation of resins with SOP and guidance on process development / evaluations Work closely with BPG cell culture team and map ongoing molecule / process development ay key customer sites to ensure technical engagement and awareness of resin solution Support customer with high-throughput protein purification process development using Poros and CaptureSelect resin Support and guide customers in downstream process development, optimization, and scale-up manufacturing, including column packing support and CIP Map customer problems and develop solutions needed optimization of process on Poros and CaptureSelect resins Champion Poros, CS technology and applications and present data at Key conferences and events Empower customers on to new technology and NPI solutions Meet country specific design in and process development targets Education And Experience Master’s degree or Doctoral degree (Ph.D.) in biochemistry, bioengineering, biology, chemistry or related fields, preferably with some relevant industry experiences with 3 to 5 years of demonstrated ability in downstream process development or manufacturing Knowledge, Skills And Abilities Good knowledge in protein chemistry and bioprocessing Previous Field based application support experience. Good knowledge and hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology; TFF Experiences in using AKTA line of purification instruments Experiences in using ultrafiltration/diafiltration instrument for buffer exchange, product concentration, and formulation Experiences in protein analysis such as HPLC, CGE, ELISA, etc. is a plus Good verbal and written communication skills, organized, coordinated, independent, meticulous Ability to multitask on different projects and work with multiple customers locally, regionally & globally Able to perform successfully under pressure while prioritizing and handling multiple projects or activities Ability to travel extensively and provide sustained customer support Benefits We offer attractive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Apply today http://jobs.thermofisher.com. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions Job Description About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Role: Bioproduction Group, Purification and Pharma Analytics division is seeking a motivated and dedicated protein purification Field Application scientist to support Poros and CaptureSelect (CS) resin design in, optimization and troubleshooting at Downstream purification and process development primarily for novel therapeutic monoclonal antibody products including bispecifics, Vaccines and general bioprocessing throughout all stages of clinical trials at key bioprocessing customer sites in India. Responsibility Conduct routine Knowledge culture seminars to highlight Poros and CS resin technology and application at key customer sites Initiate and support customer evaluation of resins with SOP and guidance on process development / evaluations Work closely with BPG cell culture team and map ongoing molecule / process development ay key customer sites to ensure technical engagement and awareness of resin solution Support customer with high-throughput protein purification process development using Poros and CaptureSelect resin Support and guide customers in downstream process development, optimization, and scale-up manufacturing, including column packing support and CIP Map customer problems and develop solutions needed optimization of process on Poros and CaptureSelect resins Champion Poros, CS technology and applications and present data at Key conferences and events Empower customers on to new technology and NPI solutions Meet country specific design in and process development targets Education and Experience Master’s degree or Doctoral degree (Ph.D.) in biochemistry, bioengineering, biology, chemistry or related fields, preferably with some relevant industry experiences with 3 to 5 years of demonstrated ability in downstream process development or manufacturing Knowledge, Skills and Abilities: Good knowledge in protein chemistry and bioprocessing Previous Field based application support experience. Good knowledge and hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology; TFF Experiences in using AKTA line of purification instruments Experiences in using ultrafiltration/diafiltration instrument for buffer exchange, product concentration, and formulation Experiences in protein analysis such as HPLC, CGE, ELISA, etc. is a plus Good verbal and written communication skills, organized, coordinated, independent, meticulous Ability to multitask on different projects and work with multiple customers locally, regionally & globally Able to perform successfully under pressure while prioritizing and handling multiple projects or activities Ability to travel extensively and provide sustained customer support BENEFITS We offer attractive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Apply today http://jobs.thermofisher.com. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Work Schedule Standard (Mon-Fri) Environmental Conditions Various outside weather conditions About Company : Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Role: Bioproduction Group, Purification and Pharma Analytics division is seeking a motivated and dedicated protein purification Field Application scientist to support Poros and CaptureSelect (CS) resin design in, optimization and troubleshooting at Downstream purification and process development primarily for novel therapeutic monoclonal antibody products including bispecifics, Vaccines and general bioprocessing throughout all stages of clinical trials at key bioprocessing customer sites in India. Responsibility Conduct routine Knowledge culture seminars to highlight Poros and CS resin technology and application at key customer sites Initiate and support customer evaluation of resins with SOP and guidance on process development / evaluations Work closely with BPG cell culture team and map ongoing molecule / process development ay key customer sites to ensure technical engagement and awareness of resin solution Support customer with high-throughput protein purification process development using Poros and CaptureSelect resin Support and guide customers in downstream process development, optimization, and scale-up manufacturing, including column packing support and CIP Map customer problems and develop solutions needed optimization of process on Poros and CaptureSelect resins Champion Poros, CS technology and applications and present data at Key conferences and events Empower customers on to new technology and NPI solutions Meet country specific design in and process development targets Education And Experience Master’s degree or Doctoral degree (Ph.D.) in biochemistry, bioengineering, biology, chemistry or related fields, preferably with some relevant industry experiences with 3 to 5 years of demonstrated ability in downstream process development or manufacturing Knowledge, Skills and Abilities: Good knowledge in protein chemistry and bioprocessing Previous Field based application support experience. Good knowledge and hands-on experiences in various types of column/membrane chromatography (affinity, size exclusion, ion exchanges, multi-mode) and filtration technology; TFF Experiences in using AKTA line of purification instruments Experiences in using ultrafiltration/diafiltration instrument for buffer exchange, product concentration, and formulation Experiences in protein analysis such as HPLC, CGE, ELISA, etc. is a plus Good verbal and written communication skills, organized, coordinated, independent, meticulous Ability to multitask on different projects and work with multiple customers locally, regionally & globally Able to perform successfully under pressure while prioritizing and handling multiple projects or activities Ability to travel extensively and provide sustained customer support Benefits We offer attractive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds have a unique story to tell. Apply today http://jobs.thermofisher.com. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Woxsen University seeks an accomplished Research Professor of Biomedical Engineering to lead cutting-edge research initiatives at the intersection of engineering and medical sciences. The successful candidate will drive innovative research programs focused on developing biomedical technologies, medical devices, and therapeutic solutions that address critical healthcare challenges. Key Responsibilities Research & Innovation: Lead and develop world-class research programs in biomedical engineering with focus on medical applications Secure external funding through grants from national and international agencies (DST, DBT, NIH, NSF, etc.) Establish and manage state-of-the-art research laboratories Collaborate with medical institutions, hospitals, and healthcare organizations Mentor doctoral and post-doctoral researchers Publish high-impact research in peer-reviewed journals and present at international conferences Academic Excellence: Teach graduate and undergraduate courses in biomedical engineering Develop innovative curriculum aligned with industry needs and emerging technologies Supervise PhD dissertations and master's theses Contribute to program development and accreditation activities Industry & Clinical Partnerships: Foster collaborations with medical device companies and pharmaceutical industries Engage in technology transfer and commercialization activities Participate in clinical trials and translational research initiatives Serve on advisory boards and professional committees Required Qualifications PhD in Biomedical Engineering, Bioengineering, or closely related field Minimum 8-10 years of post-doctoral research experience Strong publication record with H-index of 15+ and 50+ peer-reviewed publications Demonstrated success in securing research funding (minimum ₹5 crores in grants) Experience in medical device development or therapeutic technologies Proven track record of mentoring graduate students and postdoctoral fellows

As an Insights Analyst you will be required to address the following: Collaborate in the fulfillment of consulting projects with a special focus on global markets. This will require working closely with other consultants and project managers located in any of our global offices Conduct primary research with healthcare professionals, industry players as well as industry associations, and national agencies Conduct secondary research on large data sets from various data sources Collaborate in the analysis of quantitative and qualitative data for the development of financial models (i.e. eNPV), market models, economic impact models, health-economic models, as well as product adoption and acceptance models Clean, transform, and standardize complex datasets from multiple sources—including EMR, medical and pharmacy claims, and large prescription and healthcare datasets—to ensure consistency and reliability in analysis Design and develop interactive dashboards and reports using Excel and visualization tools (e.g., Power BI, Tableau) to communicate actionable insights to cross-functional team Develop market landscape presentations, market entry strategies, product positioning strategies, and others Work to solve complex business problems Participate in meetings and presentations to clients across the globe Engage in regular global training modules and required Pharmacovigilance training (internal and client-specific) Qualifications A minimum of 2-3 years of demonstrable experience within the healthcare industry in roles related to market insights/analytics, product management, strategy consulting or related roles Education: Master’s degree in Biotechnology, Pharmacy (MPharm), Bioengineering/Biomedical Engineering, Business Administration, or a related field Marketing, management consulting and/or market research, and reimbursement/pricing expertise are a plus Flexibility to work within a multicultural interdisciplinary team across various time zones Fluent in English and preferably speak other foreign languages. Self-motivated with exceptional organizational skills Advanced degree (PhD) a plus